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research Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood

12 citations , March 2012 in “JEADV. Journal of the European Academy of Dermatology and Venereology/Journal of the European Academy of Dermatology and Venereology”

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

research A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix

3 citations , February 2011 in “Journal of Biomedical Research/Journal of biomedical research”

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

research Cronkhite–Canada syndrome: from clinical features to treatment

19 citations , August 2020 in “Gastroenterology report”

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

research Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure

30 citations , August 1984 in “Journal of the American Academy of Dermatology”

Low-sulfur hair syndrome can cause UVB sensitivity and testicular failure.

Psychopharmacological Treatment of Trichotillomania in an Adolescent Case: Significant Improvement with Aripiprazole Augmentation

research Psychopharmacological Treatment of Trichotillomania in an Adolescent Case: Significant Improvement with Aripiprazole Augmentation

1 citations , December 2014 in “Klinik Psikofarmakoloji Bülteni-Bulletin of Clinical Psychopharmacology”

Adding aripiprazole to the treatment improved hair-pulling symptoms in a teenager.

research Reticular Erythematous Mucinosis Syndrome

6 citations , June 1986 in “The Journal of Dermatology”

Reticular erythematous mucinosis syndrome can occur with minimal mucin deposition.

research Pili Torti: A Feature of Numerous Congenital and Acquired Conditions

9 citations , August 2021 in “Journal of clinical medicine”

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

research Dermoscopic Findings and Their Therapeutic Implications in Trichostasis Spinulosa: A Retrospective Study of 306 Patients

13 citations , January 2018 in “Skin Appendage Disorders”

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

research The Tumor Necrosis Factor-α Level in Platelet-Rich Plasma Might Be Associated with Treatment Outcome in Patients with Interstitial Cystitis/Bladder Pain Syndrome or Recurrent Urinary Tract Infection

8 citations , December 2023 in “International Journal of Molecular Sciences”

Lower TNF-α levels in PRP may predict better treatment outcomes for bladder conditions.

research A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?

9 citations , October 1995 in “Clinical Dysmorphology”

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

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